A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7694



Internal ID9629633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143450682..143883311hg38UCSC Ensembl
Innerchr7:143147775..143580404hg19UCSC Ensembl
Innerchr7:142857897..143211337hg18UCSC Ensembl
Innerchr7:142664612..143018052hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38432630
hg19432630
hg18353441
hg17353441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758138
Supporting Variants
SamplesNA18633
Known GenesCTAGE15, CTAGE6, EPHA1-AS1, FAM115A, FAM115C, LOC154761, TAS2R41
MethodBAC aCGH
AnalysisArray images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).
PlatformAgilent
Comments
ReferenceRedon_et_al_2006
Pubmed ID17122850
Accession Number(s)essv7694
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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